5464-72-2

Basic information

• Product Name: ethyl 3-hydroxy-3-methyl-nonanoate
• Synonyms: ethyl 3-hydroxy-3-methyl-nonanoate
• CAS NO: 5464-72-2
• Molecular Formula: C₁₂H₂₄O₃
• Molecular Weight: 0
• Mol File: 5464-72-2.mol
• Article Data: 6

Chemical Properties

• Boiling Point: 306°Cat760mmHg
• Flash Point: 117.9°C
• Appearance: /
• Density: 0.95g/cm³
• Vapor Pressure: 7.4E-05mmHg at 25°C
• Refractive Index: 1.447
• CAS DataBase Reference: ethyl 3-hydroxy-3-methyl-nonanoate(CAS DataBase Reference)
• NIST Chemistry Reference: ethyl 3-hydroxy-3-methyl-nonanoate(5464-72-2)
• EPA Substance Registry System: ethyl 3-hydroxy-3-methyl-nonanoate(5464-72-2)

Safety Data

• Hazardous Substances Data: 5464-72-2(Hazardous Substances Data)

Usage

InChI:InChI=1/C12H24O3/c1-4-6-7-8-9-12(3,14)10-11(13)15-5-2/h14H,4-10H2,1-3H3

Upstream product

• 111-13-7 hexyl-methyl-ketone 
• 623-48-3 ethyl iodoacetae 
• 105-39-5 chloroacetic acid ethyl ester 
• 141-78-6 ethyl acetate 
• 73303-68-1 1-ethoxy-1-(triethylsiloxy)ethylene 
• 105-36-2 ethyl bromoacetate 

Downstream Products

• 5350-11-8 ethyl 3-methylnon-2-enoate 
• 97030-00-7 5-methyl-undecanoic acid 
• 35205-79-9 3-methylnonanoic acid 
• 91342-02-8 3-methyl-1-bromononane 
• 35205-77-7 3-methyl-non-3-enoic acid 
• 35205-76-6 3-methyl-non-2-enoic acid 
• 68329-37-3 1-(toluene-p-sulphonyloxy)-3-methylnonan-3-ol 

Relevant articles and documents

New application of bromotrimethylsilane: Elaboration of aldehydes/ketones into homologous α,β-unsaturated esters via β-hydroxy esters

α,β-Unsaturated esters are formed when β-hydroxy esters react with bromotrimethylsilane which is generated from chlorotrimethylsilane- lithium bromide in acetonitrile. Copyright Taylor & Francis, Inc.

ACTIVATION OF KETENE SILYL ACETALS BY 10-METHYLACRIDINIUM PERCHLORATE: A NOVEL CATALYSIS IN MUKAIYAMA REACTION

10-Methylacridinium perchlorate (1) effectively promotes various reactions of ketene silyl acetals: aldol and Michael addition products are obtained with aldehydes, ketones, acetals, and α-enones.The reactions exhibit unusual dependency upon 1, namely the yields are excellent when a catalytic amount of 1 is employed whereas no desired products are accessible by the use of 1 in a stoichiometric quantity.A novel catalytic cycle is proposed.

1,2-Disubstituted oxo triazolidine

Compounds of the formula (I): STR1 wherein n is 3 to 5; Y is --CH2 --CH2, --CH=CH-- or C C--; L is O or S; R1 is C1-4 alkyl; R2 is hydrogen, C1-4 alkyl or phenyl; R3 is hydroxy o